Canonical Allele Identifier: CA923740929
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs1603548769

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004649C>T , CM000686.2:g.20004649C>T GRCh38
NC_000024.9:g.22166535C>T , CM000686.1:g.22166535C>T GRCh37
NC_000024.8:g.20625923C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1091G>A